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Graves' Disease

What is Graves' Disease?

Graves' Disease is a rare thyroid disorder characterized by goitre, exophthalmos, and hyperthyroidism.

 

Graves' Disease is a rare thyroid disorder characterized by goitre, exophthalmos, and hyperthyroidism.
Acknowledgement of Graves' Disease has not been added yet.
Prevalence Information of Graves' Disease has not been added yet.
Synonyms for Graves' Disease has not been added yet.
Cause of Graves' Disease has not been added yet.
There are a number of symptoms that effect patients with Graves' Disease.
Name Description
Muscular weakness Muscular weakness
Rapid heart rate Rapid heart rate
Exophthalmos Exophthalmos is the protuberance of one or both eyes.
Fatigue Fatigue
Weight Loss Weight Loss
Hair Loss Hair Loss
Diagnosis of Graves' Disease has not been added yet.
Diagnostic tests of Graves' Disease has not been added yet
Treatments of Graves' Disease has not been added yet.
Prognosis of Graves' Disease has not been added yet.
Tips or Suggestions of Graves' Disease has not been added yet.
References of Graves' Disease has not been added yet.
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Community External News Link
Title Date Link
Graves' Disease Explained: Causes Symptoms, And Treatment 12/03/2022
Community Resources
Title Description Date Link
National Graves' Disease Foundation

The purpose of this website is to provide a resource on the world wide web for those with Graves’ disease (and others interested) to access NGDF information and materials, our online support bulletin board, NGDF membership registration, and annual Bridge to Wellness Conference information and registration.

03/20/2017

Clinical Trials


Cords registry

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access.

Enrolling is easy.

  1. Complete the screening form.
  2. Review the informed consent.
  3. Answer the permission and data sharing questions.

After these steps, the enrollment process is complete. All other questions are voluntary. However, these questions are important to patients and their families to create awareness as well as to researchers to study rare diseases. This is why we ask our participants to update their information annually or anytime changes to their information occur.

Researchers can contact CoRDS to determine if the registry contains participants with the rare disease they are researching. If the researcher determines there is a sufficient number of participants or data on the rare disease of interest within the registry, the researcher can apply for access. Upon approval from the CoRDS Scientific Advisory Board, CoRDS staff will reach out to participants on behalf of the researcher. It is then up to the participant to determine if they would like to join the study.

Visit sanfordresearch.org/CoRDS to enroll.

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Community User List

I have Graves Disease over size heart valve cyst on kidney 4 cyst in each breast tremors depression and anixtey asthma COPD arthritis in lumbar spine pinch nerve in left hand white matter disease...

Graves eye diease, dupuytrens and ledderhose
My daughter is 10 and she was diagnosed with this disorder she is currently waiting a kidney transplant and we are trying to find foundations and support groups. any help?
Diagnosis Graves Disease - Dr said well its MAJOR....

 

 

Military Wife 18+ years

 

Mom of Teenager.

 

 

Struggling with Hyperthryoidism and Graves Disease - Meds are not...
My 4 year old daughter was just diagnosed with Graves Disease. This is very rare for a child of this age. I am looking to connect with others who may have experience with this.

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